A two-phase Phase 3 study of the safety and efficacy of Sativex®, in the symptomatic relief of spasticity in subjects with spasticity due to multiple sclerosis: Phase A – single blind response assessment; Phase B - double blind, randomised, placebo controlled, parallel group study.

CompletedPhase 3MS (type not specified)2006-005910-11

What was tested

Treatment tested

  • Nabiximols

What it measured

Main measures

  • The primary endpoint is the mean spasticity NRS score over the last seven days of the evaluable period (end of treatment - usually week 17 in those subjects who demonstrated a response in Phase A.

    Spasticity

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Related trials

History

  1. In scope changed from true to false
  1. Started

    Jul 2007

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